A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706255



Internal ID19004536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126409190..126508964hg38UCSC Ensembl
Innerchr10:128097759..128197533hg19UCSC Ensembl
Innerchr10:128087749..128187523hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3899775
hg1999775
hg1899775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035647
Supporting Variants
Samples
Known GenesC10orf90, LINC00601
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3706255
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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